General Information

MaintermTEREPHTHALOYL CHLORIDE
CAS Reg.No.(or other ID)100-20-9
Regnum 177.2550
177.1585
177.1632

From www.fda.gov

Computed Descriptors

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2D Structure
CID7488
IUPAC Namebenzene-1,4-dicarbonyl chloride
InChIInChI=1S/C8H4Cl2O2/c9-7(11)5-1-2-6(4-3-5)8(10)12/h1-4H
InChI KeyLXEJRKJRKIFVNY-UHFFFAOYSA-N
Canonical SMILESC1=CC(=CC=C1C(=O)Cl)C(=O)Cl
Molecular FormulaC8H4Cl2O2
Wikipediaterephthaloyl chloride

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight203.018
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count2
Rotatable Bond Count2
Complexity173.0
CACTVS Substructure Key Fingerprint A A A D c Y B w M A A G A A A A A A A A A A A A A A A A A A A A A A A w A A A A A A A A A A A B A A A A G g I A A A A A D A K A m A A w A I A A A A C I A m B a A A A C A A A k A A A I i A E A A s g I I D K B F R C A I Q A g g A A I i Y c I i A C O Q A A A A A A A A A C A A A A A A A A A A A A A A A A A A A = =
Topological Polar Surface Area34.1
Monoisotopic Mass201.959
Exact Mass201.959
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count12
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.9856
Human Intestinal AbsorptionHIA+1.0000
Caco-2 PermeabilityCaco2+0.8554
P-glycoprotein SubstrateNon-substrate0.8582
P-glycoprotein InhibitorNon-inhibitor0.9689
Non-inhibitor0.9837
Renal Organic Cation TransporterNon-inhibitor0.8896
Distribution
Subcellular localizationMitochondria0.8256
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8137
CYP450 2D6 SubstrateNon-substrate0.9128
CYP450 3A4 SubstrateNon-substrate0.7685
CYP450 1A2 InhibitorInhibitor0.6127
CYP450 2C9 InhibitorNon-inhibitor0.8546
CYP450 2D6 InhibitorNon-inhibitor0.9073
CYP450 2C19 InhibitorNon-inhibitor0.6533
CYP450 3A4 InhibitorNon-inhibitor0.9178
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.9189
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9480
Non-inhibitor0.9738
AMES ToxicityAMES toxic0.9251
CarcinogensCarcinogens 0.5000
Fish ToxicityHigh FHMT0.8531
Tetrahymena Pyriformis ToxicityHigh TPT0.9995
Honey Bee ToxicityHigh HBT0.6691
BiodegradationNot ready biodegradable0.5803
Acute Oral ToxicityIII0.8874
Carcinogenicity (Three-class)Non-required0.7836

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility-2.5196LogS
Caco-2 Permeability1.8726LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity1.9003LD50, mol/kg
Fish Toxicity-0.1277pLC50, mg/L
Tetrahymena Pyriformis Toxicity1.0751pIGC50, ug/L

From admetSAR


Taxonomic Classification

KingdomOrganic compounds
SuperclassBenzenoids
ClassBenzene and substituted derivatives
SubclassBenzoic acids and derivatives
Intermediate Tree NodesNot available
Direct ParentBenzoic acids and derivatives
Alternative Parents
Molecular FrameworkAromatic homomonocyclic compounds
SubstituentsBenzoic acid or derivatives - Benzoyl - Acyl halide - Acyl chloride - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as benzoic acids and derivatives. These are organic compounds containing a carboxylic acid substituent attached to a benzene ring.

From ClassyFire